ZMP
timm17a
Ensembl ID:
ZFIN ID:
Description:
mitochondrial import inner membrane translocase subunit Tim17-A [Source:RefSeq peptide;Acc:NP_93818
Human Orthologue:
TIMM17A
Human Description:
translocase of inner mitochondrial membrane 17 homolog A (yeast) [Source:HGNC Symbol;Acc:17315]
Mouse Orthologue:
Timm17a
Mouse Description:
translocase of inner mitochondrial membrane 17a Gene [Source:MGI Symbol;Acc:MGI:1343131]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2587 | Nonsense | F2 line generated | Not yet available |
| sa35084 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2587
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044987 | None | None | 166 | None | 6 |
| ENSDART00000127976 | Nonsense | 18 | 201 | 1 | 6 |
The following transcripts of ENSDARG00000029510 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 25833773)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 24662598 |
| GRCz11 | 11 | 24900214 |
KASP Assay ID:
554-2573.1 (used for ordering genotyping assays)
KASP Sequence:
GTTCRCACAGAAAGAACCAGCGAAAAACGCACGAGGAACCTTACGTCACT[T/A]GCAGCAACAGCACGTGCTTGGTTACGTCAGTTGTGAACGGGAAAAGAACA
Long Flanking Sequence:
TTATGATTTTAAATTTGTACTTACCATCAGAATGGTTTCAAGGTAAAAAAATAAAATAATGCTACATTATGATTATGTGTTGGCAGTTAAAACATTTATTAGAAATTTCGAAATGTTATTAAAAAAACACCATCAGTTACATTACTTTCAAAAAGCACTTAAATTAATTAGGTACAACTTTAAATATTGTAACTTGTGATCTTTCTTAAAACTTTAAACCATGAGCAAAAGATCACAAAGATCTATTTTTTCACCTTTGTTGTTCATAGTGAAAAGAGGAGTCCTCGTAAACTAGAATACTCCCAAGTCTCAGCTGCCGGCAAACGAATGACAACGTCGCGCACCTCTGATGATATATGATAATGATAATATATAATTGAGTCACATTTTTTGACTTTGAATGGTTTGGTGGTTGTAAAACTTCCTCCACTAGAGGGGCGTCTTTGCAATGTTCACACAGAAAGAACCAGCGAAAAACGCACGAGGAACCTTACGTCACT[T/A]GCAGCAACAGCACGTGCTTGGTTACGTCAGTTGTGAACGGGAAAAGAACAAAATGGAGGAGTACGCGAGGGAGCCGTGGTGAGCCGACAGCCTCAAACCTATTATTTTATACGTTCAGTGAATTTATATGGTTTTATTTCTCTAACGGTCATACTGTAGTATGTTATTTCTACGCTGTAATTAATTGTCAGGGTGTCTGACGCTCGCAATATTGTGATATGGTGGTTTTGATGGAGTTTTTTTTAACACGATGCCCTTCAGTGAAGGCTTCATGCTGTCAGTGCCGCACATGACCTTGTTCTACCGGCTTCAGAGATCACTAGATTTTGTTTTTGTATAATGTCTTCCAGAAATGTCTGTTGTGTAAATTCGTCGACTGTTAAACGCAGATTATAGATTACAATATACGTAACAGTTATGCTTGCTGGTTTCTGCAAATCACCTGGGTAGCCTTACGGTAAATAACTATGTAGTTATGAAGTAACTATGTACAATGTAAT
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa35084
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044987 | Nonsense | 4 | 166 | 1 | 6 |
| ENSDART00000127976 | Nonsense | 39 | 201 | 1 | 6 |
The following transcripts of ENSDARG00000029510 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 11 (position 25833837)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 24662662 |
| GRCz11 | 11 | 24900278 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTTGGTTACGTCAGTTGTGAACGGGAAAAGAACAAAATGGAGGAGTA[C/A]GCGAGGGAGCCGTGGTGAGCCGACAGCCTCAAACCTATTATTTTATACGT
Long Flanking Sequence:
CATTATGATTATGTGTTGGCAGTTAAAACATTTATTAGAAATTTCGAAATGTTATTAAAAAAACACCATCAGTTACATTACTTTCAAAAAGCACTTAAATTAATTAGGTACAACTTTAAATATTGTAACTTGTGATCTTTCTTAAAACTTTAAACCATGAGCAAAAGATCACAAAGATCTATTTTTTCACCTTTGTTGTTCATAGTGAAAAGAGGAGTCCTCGTAAACTAGAATACTCCCAAGTCTCAGCTGCCGGCAAACGAATGACAACGTCGCGCACCTCTGATGATATATGATAATGATAATATATAATTGAGTCACATTTTTTGACTTTGAATGGTTTGGTGGTTGTAAAACTTCCTCCACTAGAGGGGCGTCTTTGCAATGTTCACACAGAAAGAACCAGCGAAAAACGCACGAGGAACCTTACGTCACTTGCAGCAACAGCACGTGCTTGGTTACGTCAGTTGTGAACGGGAAAAGAACAAAATGGAGGAGTA[C/A]GCGAGGGAGCCGTGGTGAGCCGACAGCCTCAAACCTATTATTTTATACGTTCAGTGAATTTATATGGTTTTATTTCTCTAACGGTCATACTGTAGTATGTTATTTCTACGCTGTAATTAATTGTCAGGGTGTCTGACGCTCGCAATATTGTGATATGGTGGTTTTGATGGAGTTTTTTTTAACACGATGCCCTTCAGTGAAGGCTTCATGCTGTCAGTGCCGCACATGACCTTGTTCTACCGGCTTCAGAGATCACTAGATTTTGTTTTTGTATAATGTCTTCCAGAAATGTCTGTTGTGTAAATTCGTCGACTGTTAAACGCAGATTATAGATTACAATATACGTAACAGTTATGCTTGCTGGTTTCTGCAAATCACCTGGGTAGCCTTACGGTAAATAACTATGTAGTTATGAAGTAACTATGTACAATGTAATAACCGTGTTTGGTCCTATTGATCACTGTTGGTTTTATCAGATATGCAACAGGCAAACTATTTTA
Associated Phenotype:
Not determined